UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Evaluation of soluble fibrin monomer complex in patients in SARS‐CoV‐2 COVID‐19 infection‐associated coagulopathy

European journal of haematology, 2022-04, Vol.108 (4), p.319-326

2022

Volltextzugriff (PDF)

Germline Mutations in NFKB2 Implicate the Noncanonical NF-κB Pathway in the Pathogenesis of Common Variable Immunodeficiency

American journal of human genetics, 2013-11, Vol.93 (5), p.812-824

2013

Volltextzugriff (PDF)

Off-the-shelf cryopreserved platelets for the detection of HIT and VITT antibodies

Blood, 2022-12, Vol.140 (25), p.2722-2729

2022

Volltextzugriff (PDF)

Rare complication of treated immune thrombocytopenia

American journal of hematology, 2017-11, Vol.92 (11), p.1262-1266

2017

Volltextzugriff (PDF)

Protein S testing in patients with protein S deficiency, factor V Leiden, and rivaroxaban by North American Specialized Coagulation Laboratories

Thrombosis and haemostasis, 2016-07, Vol.116 (1), p.50-57

2016

Volltextzugriff (PDF)

Laboratory testing for platelet antibodies

American journal of hematology, 2013-09, Vol.88 (9), p.818-821

2013

Volltextzugriff (PDF)

“Autoimmune HIT” antibodies in diagnostic samples are a potential artifact and not associated with more severe outcomes

Blood advances, 2023-08, Vol.7 (16), p.4431-4434

2023

Volltextzugriff (PDF)

Elevated factor IX activity is associated with an increased odds ratio for both arterial and venous thrombotic events

American journal of clinical pathology, 2013-11, Vol.140 (5), p.680-685

2013

Volltextzugriff (PDF)

Spindle cell variant of multiple myeloma: immunophenotype and cytogenetics abnormalities

Annals of hematology, 2012-05, Vol.91 (5), p.803-804

2012

Volltextzugriff (PDF)

Neoplastic plasma cell aberrant antigen expression patterns and their association with genetic abnormalities

Leukemia & lymphoma, 2015-02, Vol.56 (2), p.426-433

2015

Volltextzugriff (PDF)

Evaluation of Soluble Fibrin Monomer Complex in Patients with Sars-Cov-2 COVID-19 Infection

Blood, 2020-11, Vol.136 (Supplement 1), p.27-28

2020

Volltextzugriff (PDF)

Thrombophilia Testing Practices: The Mayo Clinic Experience

Blood, 2020-11, Vol.136 (Supplement 1), p.39-40

2020

Volltextzugriff (PDF)

A Thrombospondin-1 Release Assay (TRA) Coupled to PF4-Treated Cryopreserved Platelets for the Detection of Pathogenic HIT and VITT Antibodies

Blood, 2021-11, Vol.138 (Supplement 1), p.2130-2130

2021

Volltextzugriff (PDF)

Determination of Relapse Risk By Complement Gene Variants after Eculizumab Discontinuation in Complement-Mediated Thrombotic Microangiopathy: A Retrospective Review

Blood, 2020-11, Vol.136 (Supplement 1), p.25-26

2020

Volltextzugriff (PDF)

Germline Mutations in NFKB2 Implicate the Noncanonical NF-[kappa]B Pathway in the Pathogenesis of Common Variable Immunodeficiency

American journal of human genetics, 2013-11, Vol.93 (5), p.812

2013

Volltextzugriff (PDF)

Neoplastic plasma cell aberrant antigen expression patterns and their association with genetic abnormalities

Leukemia & Lymphoma, 2015, Vol.56 (2), p.426-433

2015

Volltextzugriff (PDF)

Pregnancy characteristics in Egyptian female patients with NMOSD

Multiple sclerosis journal - experimental, translational and clinical, 2024-07, Vol.10 (3), p.20552173241271878

2024

Volltextzugriff (PDF)

Acute Intermittent Porphyria as a Rare Challenging Neuro-Metabolic Disease; a Case Report

Archives of academic emergency medicine, 2022-01, Vol.10 (1)

2022

Volltextzugriff (PDF)

Deparaffinization with mineral oil: a simple procedure for extraction of high-quality DNA from archival formalin-fixed paraffin-embedded samples

Applied immunohistochemistry & molecular morphology, 2014-09, Vol.22 (8), p.623-626

2014

Volltextzugriff (PDF)

Improved harmonization of eosin-5-maleimide binding test across different instruments and age groups

Cytometry. Part B, Clinical cytometry, 2016-11, Vol.90 (6), p.512-516

2016

Volltextzugriff (PDF)

Evaluation of Mass Cytometry in the Clinical Laboratory

Cytometry. Part B, Clinical cytometry, 2019-07, Vol.96 (4), p.266-274

2019

Volltextzugriff (PDF)

Acute Intermittent Porphyria as a Rare Challenging Neuro-Metabolic Disease; a Case Report

Archives of academic emergency medicine, 2022, Vol.10 (1), p.e74-e74

2022

Volltextzugriff (PDF)

1 – 23 von 23

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(19)
Mit Volltextzugriff
(19)

Publikationsform

Artikel
(21)
Berichte
(2)

Sprache

Englisch
(23)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Evaluation of soluble fibrin monomer complex in patients in SARS‐CoV‐2 COVID‐19 infection‐associated coagulopathy

Germline Mutations in NFKB2 Implicate the Noncanonical NF-κB Pathway in the Pathogenesis of Common Variable Immunodeficiency

Off-the-shelf cryopreserved platelets for the detection of HIT and VITT antibodies

Rare complication of treated immune thrombocytopenia

Protein S testing in patients with protein S deficiency, factor V Leiden, and rivaroxaban by North American Specialized Coagulation Laboratories

Laboratory testing for platelet antibodies

“Autoimmune HIT” antibodies in diagnostic samples are a potential artifact and not associated with more severe outcomes

Elevated factor IX activity is associated with an increased odds ratio for both arterial and venous thrombotic events

Spindle cell variant of multiple myeloma: immunophenotype and cytogenetics abnormalities

Neoplastic plasma cell aberrant antigen expression patterns and their association with genetic abnormalities

Evaluation of Soluble Fibrin Monomer Complex in Patients with Sars-Cov-2 COVID-19 Infection

Thrombophilia Testing Practices: The Mayo Clinic Experience

A Thrombospondin-1 Release Assay (TRA) Coupled to PF4-Treated Cryopreserved Platelets for the Detection of Pathogenic HIT and VITT Antibodies

Determination of Relapse Risk By Complement Gene Variants after Eculizumab Discontinuation in Complement-Mediated Thrombotic Microangiopathy: A Retrospective Review

Germline Mutations in NFKB2 Implicate the Noncanonical NF-[kappa]B Pathway in the Pathogenesis of Common Variable Immunodeficiency

Neoplastic plasma cell aberrant antigen expression patterns and their association with genetic abnormalities

Pregnancy characteristics in Egyptian female patients with NMOSD

Acute Intermittent Porphyria as a Rare Challenging Neuro-Metabolic Disease; a Case Report

Deparaffinization with mineral oil: a simple procedure for extraction of high-quality DNA from archival formalin-fixed paraffin-embedded samples

Improved harmonization of eosin-5-maleimide binding test across different instruments and age groups

Evaluation of Mass Cytometry in the Clinical Laboratory

Complement gene variant effect on relapse of complement-mediated thrombotic microangiopathy after eculizumab cessation

Acute Intermittent Porphyria as a Rare Challenging Neuro-Metabolic Disease; a Case Report

Suchergebnisse filtern